| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9240318-9240394 | Common:1; Rare:16 | ||||
| chr12:9448179-9448301 | Common:1; Rare:61 | ||||
| chr12:9648021-9648362 | Common:4; Rare:105 | ||||
| chr12:11016042-11016077 | Rare:5 | ||||
| chr12:12999267-12999506 | Common:1; Rare:42 | ||||
| chr12:14625874-14626156 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
| chr12:14639893-14640178 | Rare:61; Clinvar (pathogenic):1 | ||||
| chr12:15746463-15746508 | Rare:9 | ||||
| chr12:20405428-20405665 | Common:1; Rare:36 | ||||
| chr12:20420373-20420695 | Common:2; Rare:56 | ||||
| chr12:39946166-39946482 | Common:1; Rare:45 | ||||
| chr12:43951911-43951997 | Common:1; Rare:21 | ||||
| chr12:45727440-45727813 | Rare:155 | ||||
| chr12:46383951-46384071 | Common:1; Rare:32 | ||||
| chr12:47857653-47857916 | Common:2; Rare:61; Clinvar:1 |